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You searched for +publisher:"University of Toronto" +contributor:("Bapat, Bharati"). Showing records 1 – 12 of 12 total matches.

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University of Toronto

1. Ho, Linh Thuy. Genome-wide Distribution and Regulation of DNA Methylation and Hydroxymethylation in Prostate Cancer.

Degree: 2014, University of Toronto

Prostate cancer (PCa) is the most common malignancy in men. Epigenetic alterations, including DNA methylation, significantly influence disease pathogenesis. Aberrant methylation of the cytosine base… (more)

Subjects/Keywords: DNA hydroxymethylation; DNA methylation; Epigenetics; Next-generation sequencing; Prostate cancer; TET proteins; 0715

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APA (6th Edition):

Ho, L. T. (2014). Genome-wide Distribution and Regulation of DNA Methylation and Hydroxymethylation in Prostate Cancer. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/70772

Chicago Manual of Style (16th Edition):

Ho, Linh Thuy. “Genome-wide Distribution and Regulation of DNA Methylation and Hydroxymethylation in Prostate Cancer.” 2014. Masters Thesis, University of Toronto. Accessed September 19, 2020. http://hdl.handle.net/1807/70772.

MLA Handbook (7th Edition):

Ho, Linh Thuy. “Genome-wide Distribution and Regulation of DNA Methylation and Hydroxymethylation in Prostate Cancer.” 2014. Web. 19 Sep 2020.

Vancouver:

Ho LT. Genome-wide Distribution and Regulation of DNA Methylation and Hydroxymethylation in Prostate Cancer. [Internet] [Masters thesis]. University of Toronto; 2014. [cited 2020 Sep 19]. Available from: http://hdl.handle.net/1807/70772.

Council of Science Editors:

Ho LT. Genome-wide Distribution and Regulation of DNA Methylation and Hydroxymethylation in Prostate Cancer. [Masters Thesis]. University of Toronto; 2014. Available from: http://hdl.handle.net/1807/70772


University of Toronto

2. Cuizon, Carmelle Fatima. Exploring DNA Methylation in Tumour-adjacent Normal Prostate Tissue and Evaluating its Role as a Biomarker for PCa Detection.

Degree: 2017, University of Toronto

DNA methylation alterations as a result of field cancerization may be used as diagnostic biomarkers to improve Prostate Cancer (PCa) detection. To identify diagnostic biomarkers,… (more)

Subjects/Keywords: Biomarkers; Biopsy; Diagnosis; DNA Methylation; Field Cancerization; Prostate Cancer; 0369

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APA (6th Edition):

Cuizon, C. F. (2017). Exploring DNA Methylation in Tumour-adjacent Normal Prostate Tissue and Evaluating its Role as a Biomarker for PCa Detection. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/77783

Chicago Manual of Style (16th Edition):

Cuizon, Carmelle Fatima. “Exploring DNA Methylation in Tumour-adjacent Normal Prostate Tissue and Evaluating its Role as a Biomarker for PCa Detection.” 2017. Masters Thesis, University of Toronto. Accessed September 19, 2020. http://hdl.handle.net/1807/77783.

MLA Handbook (7th Edition):

Cuizon, Carmelle Fatima. “Exploring DNA Methylation in Tumour-adjacent Normal Prostate Tissue and Evaluating its Role as a Biomarker for PCa Detection.” 2017. Web. 19 Sep 2020.

Vancouver:

Cuizon CF. Exploring DNA Methylation in Tumour-adjacent Normal Prostate Tissue and Evaluating its Role as a Biomarker for PCa Detection. [Internet] [Masters thesis]. University of Toronto; 2017. [cited 2020 Sep 19]. Available from: http://hdl.handle.net/1807/77783.

Council of Science Editors:

Cuizon CF. Exploring DNA Methylation in Tumour-adjacent Normal Prostate Tissue and Evaluating its Role as a Biomarker for PCa Detection. [Masters Thesis]. University of Toronto; 2017. Available from: http://hdl.handle.net/1807/77783


University of Toronto

3. Zhao, Fang. Exploring Urinary Epigenetic Biomarkers for Identification of Aggressive Prostate Cancer.

Degree: PhD, 2020, University of Toronto

 Prostate cancer (PCa) is the most common non-cutaneous malignancy in men. However, the majority of PCa diagnoses are localized, low-grade, clinically insignificant (CI-PCa) tumours that… (more)

Subjects/Keywords: Active Surveillance; Biomarkers; DNA methylation; miRNA; Prostate Cancer; Urine-based biomarker; 0992

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APA (6th Edition):

Zhao, F. (2020). Exploring Urinary Epigenetic Biomarkers for Identification of Aggressive Prostate Cancer. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/101205

Chicago Manual of Style (16th Edition):

Zhao, Fang. “Exploring Urinary Epigenetic Biomarkers for Identification of Aggressive Prostate Cancer.” 2020. Doctoral Dissertation, University of Toronto. Accessed September 19, 2020. http://hdl.handle.net/1807/101205.

MLA Handbook (7th Edition):

Zhao, Fang. “Exploring Urinary Epigenetic Biomarkers for Identification of Aggressive Prostate Cancer.” 2020. Web. 19 Sep 2020.

Vancouver:

Zhao F. Exploring Urinary Epigenetic Biomarkers for Identification of Aggressive Prostate Cancer. [Internet] [Doctoral dissertation]. University of Toronto; 2020. [cited 2020 Sep 19]. Available from: http://hdl.handle.net/1807/101205.

Council of Science Editors:

Zhao F. Exploring Urinary Epigenetic Biomarkers for Identification of Aggressive Prostate Cancer. [Doctoral Dissertation]. University of Toronto; 2020. Available from: http://hdl.handle.net/1807/101205


University of Toronto

4. Liu, Si Cong. Assessment of Serum MicroRNA Biomarkers for Differentiating Between Indolent and Aggressive Prostate Cancer in Active Surveillance Patients.

Degree: 2017, University of Toronto

A significant portion prostate cancer (PCa) patients on active surveillance (AS) eventually reclassifies to a higher risk-status due to occult, aggressive tumours or rapid disease… (more)

Subjects/Keywords: active surveillance; biomarker; microRNA; non-invasive; prostate cancer; 0564

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APA (6th Edition):

Liu, S. C. (2017). Assessment of Serum MicroRNA Biomarkers for Differentiating Between Indolent and Aggressive Prostate Cancer in Active Surveillance Patients. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/79211

Chicago Manual of Style (16th Edition):

Liu, Si Cong. “Assessment of Serum MicroRNA Biomarkers for Differentiating Between Indolent and Aggressive Prostate Cancer in Active Surveillance Patients.” 2017. Masters Thesis, University of Toronto. Accessed September 19, 2020. http://hdl.handle.net/1807/79211.

MLA Handbook (7th Edition):

Liu, Si Cong. “Assessment of Serum MicroRNA Biomarkers for Differentiating Between Indolent and Aggressive Prostate Cancer in Active Surveillance Patients.” 2017. Web. 19 Sep 2020.

Vancouver:

Liu SC. Assessment of Serum MicroRNA Biomarkers for Differentiating Between Indolent and Aggressive Prostate Cancer in Active Surveillance Patients. [Internet] [Masters thesis]. University of Toronto; 2017. [cited 2020 Sep 19]. Available from: http://hdl.handle.net/1807/79211.

Council of Science Editors:

Liu SC. Assessment of Serum MicroRNA Biomarkers for Differentiating Between Indolent and Aggressive Prostate Cancer in Active Surveillance Patients. [Masters Thesis]. University of Toronto; 2017. Available from: http://hdl.handle.net/1807/79211


University of Toronto

5. Rawson, James B. Methylation of Wnt Antagonist Genes and Wnt5a as Prognostic Markers in Colorectal Cancer.

Degree: 2010, University of Toronto

DKK1, SFRP1, WIF-1, and Wnt5a encode Wnt pathway genes that are frequently silenced by promoter hypermethylation in colorectal cancer. Despite attractive biological consequences of these… (more)

Subjects/Keywords: Wnt; Colorectal; Prognosis; Methylation; 0369; 0766; 0992

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APA (6th Edition):

Rawson, J. B. (2010). Methylation of Wnt Antagonist Genes and Wnt5a as Prognostic Markers in Colorectal Cancer. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/25902

Chicago Manual of Style (16th Edition):

Rawson, James B. “Methylation of Wnt Antagonist Genes and Wnt5a as Prognostic Markers in Colorectal Cancer.” 2010. Masters Thesis, University of Toronto. Accessed September 19, 2020. http://hdl.handle.net/1807/25902.

MLA Handbook (7th Edition):

Rawson, James B. “Methylation of Wnt Antagonist Genes and Wnt5a as Prognostic Markers in Colorectal Cancer.” 2010. Web. 19 Sep 2020.

Vancouver:

Rawson JB. Methylation of Wnt Antagonist Genes and Wnt5a as Prognostic Markers in Colorectal Cancer. [Internet] [Masters thesis]. University of Toronto; 2010. [cited 2020 Sep 19]. Available from: http://hdl.handle.net/1807/25902.

Council of Science Editors:

Rawson JB. Methylation of Wnt Antagonist Genes and Wnt5a as Prognostic Markers in Colorectal Cancer. [Masters Thesis]. University of Toronto; 2010. Available from: http://hdl.handle.net/1807/25902


University of Toronto

6. Liu, Li Yang. Association of Tissue Promoter Methylation Levels of APC, RASSF1A, CYP26A1, and TBX15 with Prostate Cancer Progression.

Degree: 2012, University of Toronto

Aberrant promoter methylation is known to silence tumor-suppressor genes in prostate cancer. Using a quantitative real-time PCR assay(MethyLight), I determined promoter methylation levels of APC,… (more)

Subjects/Keywords: DNA Methylation; Prostate Cancer; Epigenetic Mechanism; Progression; Biochemical Recurrence; 0369; 0307

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APA (6th Edition):

Liu, L. Y. (2012). Association of Tissue Promoter Methylation Levels of APC, RASSF1A, CYP26A1, and TBX15 with Prostate Cancer Progression. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/33724

Chicago Manual of Style (16th Edition):

Liu, Li Yang. “Association of Tissue Promoter Methylation Levels of APC, RASSF1A, CYP26A1, and TBX15 with Prostate Cancer Progression.” 2012. Masters Thesis, University of Toronto. Accessed September 19, 2020. http://hdl.handle.net/1807/33724.

MLA Handbook (7th Edition):

Liu, Li Yang. “Association of Tissue Promoter Methylation Levels of APC, RASSF1A, CYP26A1, and TBX15 with Prostate Cancer Progression.” 2012. Web. 19 Sep 2020.

Vancouver:

Liu LY. Association of Tissue Promoter Methylation Levels of APC, RASSF1A, CYP26A1, and TBX15 with Prostate Cancer Progression. [Internet] [Masters thesis]. University of Toronto; 2012. [cited 2020 Sep 19]. Available from: http://hdl.handle.net/1807/33724.

Council of Science Editors:

Liu LY. Association of Tissue Promoter Methylation Levels of APC, RASSF1A, CYP26A1, and TBX15 with Prostate Cancer Progression. [Masters Thesis]. University of Toronto; 2012. Available from: http://hdl.handle.net/1807/33724


University of Toronto

7. Kron, Kenneth James. Investigation of Novel Progression-related Methylation Events and HOXD Genes in Prostate Cancer.

Degree: 2012, University of Toronto

Aberrant DNA methylation in gene promoters causes gene silencing and is a common event in prostate cancer development and progression. While commonly identified methylated genes… (more)

Subjects/Keywords: prostate cancer; DNA methylation; homeobox; prognosis; 0992; 0369; 0307

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APA (6th Edition):

Kron, K. J. (2012). Investigation of Novel Progression-related Methylation Events and HOXD Genes in Prostate Cancer. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/34773

Chicago Manual of Style (16th Edition):

Kron, Kenneth James. “Investigation of Novel Progression-related Methylation Events and HOXD Genes in Prostate Cancer.” 2012. Doctoral Dissertation, University of Toronto. Accessed September 19, 2020. http://hdl.handle.net/1807/34773.

MLA Handbook (7th Edition):

Kron, Kenneth James. “Investigation of Novel Progression-related Methylation Events and HOXD Genes in Prostate Cancer.” 2012. Web. 19 Sep 2020.

Vancouver:

Kron KJ. Investigation of Novel Progression-related Methylation Events and HOXD Genes in Prostate Cancer. [Internet] [Doctoral dissertation]. University of Toronto; 2012. [cited 2020 Sep 19]. Available from: http://hdl.handle.net/1807/34773.

Council of Science Editors:

Kron KJ. Investigation of Novel Progression-related Methylation Events and HOXD Genes in Prostate Cancer. [Doctoral Dissertation]. University of Toronto; 2012. Available from: http://hdl.handle.net/1807/34773


University of Toronto

8. Savio, Andrea Josephine. The Dynamic Interplay of Epigenetics and Genetics in Selected DNA Mismatch Repair and Wnt Signaling Pathway Genes in Colorectal Cancer.

Degree: PhD, 2017, University of Toronto

 Colorectal cancers (CRC) undergo distinct genetic and epigenetic alterations, contributing towards chromosomal instability (CIN), microsatellite instability (MSI), and/or epigenetic instability (CpG island methylator phenotype). Two… (more)

Subjects/Keywords: Colorectal Cancer; Epigenetics; Methylation; Mismatch repair; Single nucleotide polymorphisms; 0992

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APA (6th Edition):

Savio, A. J. (2017). The Dynamic Interplay of Epigenetics and Genetics in Selected DNA Mismatch Repair and Wnt Signaling Pathway Genes in Colorectal Cancer. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/79451

Chicago Manual of Style (16th Edition):

Savio, Andrea Josephine. “The Dynamic Interplay of Epigenetics and Genetics in Selected DNA Mismatch Repair and Wnt Signaling Pathway Genes in Colorectal Cancer.” 2017. Doctoral Dissertation, University of Toronto. Accessed September 19, 2020. http://hdl.handle.net/1807/79451.

MLA Handbook (7th Edition):

Savio, Andrea Josephine. “The Dynamic Interplay of Epigenetics and Genetics in Selected DNA Mismatch Repair and Wnt Signaling Pathway Genes in Colorectal Cancer.” 2017. Web. 19 Sep 2020.

Vancouver:

Savio AJ. The Dynamic Interplay of Epigenetics and Genetics in Selected DNA Mismatch Repair and Wnt Signaling Pathway Genes in Colorectal Cancer. [Internet] [Doctoral dissertation]. University of Toronto; 2017. [cited 2020 Sep 19]. Available from: http://hdl.handle.net/1807/79451.

Council of Science Editors:

Savio AJ. The Dynamic Interplay of Epigenetics and Genetics in Selected DNA Mismatch Repair and Wnt Signaling Pathway Genes in Colorectal Cancer. [Doctoral Dissertation]. University of Toronto; 2017. Available from: http://hdl.handle.net/1807/79451


University of Toronto

9. Olkhov-Mitsel, Ekaterina. Epigenetic Analysis of the Kallikrein Gene Family and Associated Pathways as a Novel Panel of Prostate Cancer Biomarkers.

Degree: PhD, 2015, University of Toronto

Aberrant epigenetic landscape is a hallmark of prostate cancer (PCa), one of the most common cancers among men worldwide. Currently, improved understanding of the molecular… (more)

Subjects/Keywords: Biomarkers; DNA methylation; Kallikrein-related peptidases; MicroRNA; Multiplex qPCR; Prostate cancer; 0992

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APA (6th Edition):

Olkhov-Mitsel, E. (2015). Epigenetic Analysis of the Kallikrein Gene Family and Associated Pathways as a Novel Panel of Prostate Cancer Biomarkers. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/77512

Chicago Manual of Style (16th Edition):

Olkhov-Mitsel, Ekaterina. “Epigenetic Analysis of the Kallikrein Gene Family and Associated Pathways as a Novel Panel of Prostate Cancer Biomarkers.” 2015. Doctoral Dissertation, University of Toronto. Accessed September 19, 2020. http://hdl.handle.net/1807/77512.

MLA Handbook (7th Edition):

Olkhov-Mitsel, Ekaterina. “Epigenetic Analysis of the Kallikrein Gene Family and Associated Pathways as a Novel Panel of Prostate Cancer Biomarkers.” 2015. Web. 19 Sep 2020.

Vancouver:

Olkhov-Mitsel E. Epigenetic Analysis of the Kallikrein Gene Family and Associated Pathways as a Novel Panel of Prostate Cancer Biomarkers. [Internet] [Doctoral dissertation]. University of Toronto; 2015. [cited 2020 Sep 19]. Available from: http://hdl.handle.net/1807/77512.

Council of Science Editors:

Olkhov-Mitsel E. Epigenetic Analysis of the Kallikrein Gene Family and Associated Pathways as a Novel Panel of Prostate Cancer Biomarkers. [Doctoral Dissertation]. University of Toronto; 2015. Available from: http://hdl.handle.net/1807/77512


University of Toronto

10. Mrkonjic, Miralem. Evaluation of Mismatch Repair Gene Polymorphisms and their Contribution to Colorectal Cancer and its Subsets.

Degree: 2009, University of Toronto

Colorectal cancer (CRC) is a major source of morbidity and mortality in the Western world. Approximately 15% of all CRCs develop via the mutator pathway,… (more)

Subjects/Keywords: Colorectal Cancer; Mismatch Repair; Single Nucleotide Polymorphism; DNA Methylation; 0369; 0307; 0571

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APA (6th Edition):

Mrkonjic, M. (2009). Evaluation of Mismatch Repair Gene Polymorphisms and their Contribution to Colorectal Cancer and its Subsets. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/26473

Chicago Manual of Style (16th Edition):

Mrkonjic, Miralem. “Evaluation of Mismatch Repair Gene Polymorphisms and their Contribution to Colorectal Cancer and its Subsets.” 2009. Doctoral Dissertation, University of Toronto. Accessed September 19, 2020. http://hdl.handle.net/1807/26473.

MLA Handbook (7th Edition):

Mrkonjic, Miralem. “Evaluation of Mismatch Repair Gene Polymorphisms and their Contribution to Colorectal Cancer and its Subsets.” 2009. Web. 19 Sep 2020.

Vancouver:

Mrkonjic M. Evaluation of Mismatch Repair Gene Polymorphisms and their Contribution to Colorectal Cancer and its Subsets. [Internet] [Doctoral dissertation]. University of Toronto; 2009. [cited 2020 Sep 19]. Available from: http://hdl.handle.net/1807/26473.

Council of Science Editors:

Mrkonjic M. Evaluation of Mismatch Repair Gene Polymorphisms and their Contribution to Colorectal Cancer and its Subsets. [Doctoral Dissertation]. University of Toronto; 2009. Available from: http://hdl.handle.net/1807/26473


University of Toronto

11. Charames, George Shawn. Molecular Mechanisms of the Cooperation between Rac1/1b GTPases and the Canonical Wnt Signaling Pathway in Colorectal Cancer.

Degree: 2010, University of Toronto

Aberrant activation of the canonical Wnt signaling pathway accounts for the vast majority of colorectal cancers. The Rac1 GTPase is overexpressed in colon cancer, and… (more)

Subjects/Keywords: Rac1; Wnt; Colon cancer; Rac1b; 0307; 0992

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APA (6th Edition):

Charames, G. S. (2010). Molecular Mechanisms of the Cooperation between Rac1/1b GTPases and the Canonical Wnt Signaling Pathway in Colorectal Cancer. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/26158

Chicago Manual of Style (16th Edition):

Charames, George Shawn. “Molecular Mechanisms of the Cooperation between Rac1/1b GTPases and the Canonical Wnt Signaling Pathway in Colorectal Cancer.” 2010. Doctoral Dissertation, University of Toronto. Accessed September 19, 2020. http://hdl.handle.net/1807/26158.

MLA Handbook (7th Edition):

Charames, George Shawn. “Molecular Mechanisms of the Cooperation between Rac1/1b GTPases and the Canonical Wnt Signaling Pathway in Colorectal Cancer.” 2010. Web. 19 Sep 2020.

Vancouver:

Charames GS. Molecular Mechanisms of the Cooperation between Rac1/1b GTPases and the Canonical Wnt Signaling Pathway in Colorectal Cancer. [Internet] [Doctoral dissertation]. University of Toronto; 2010. [cited 2020 Sep 19]. Available from: http://hdl.handle.net/1807/26158.

Council of Science Editors:

Charames GS. Molecular Mechanisms of the Cooperation between Rac1/1b GTPases and the Canonical Wnt Signaling Pathway in Colorectal Cancer. [Doctoral Dissertation]. University of Toronto; 2010. Available from: http://hdl.handle.net/1807/26158


University of Toronto

12. Perera, Needra Sheron. Assessment of Missense Alterations in MLH1 and their Pathogenic Significance.

Degree: 2010, University of Toronto

Germline mutations in mismatch repair genes predispose individuals to Lynch Syndrome, the most common colorectal cancer predisposition syndrome. MLH1 is a key mismatch repair gene… (more)

Subjects/Keywords: Mismatch Repair; DNA repair; Cancer; Colorectal cancer; Cancer Genetics; unclassified variant; DNA alterations; Lynch syndrome; 0369; 0307; 0992

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APA (6th Edition):

Perera, N. S. (2010). Assessment of Missense Alterations in MLH1 and their Pathogenic Significance. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/32048

Chicago Manual of Style (16th Edition):

Perera, Needra Sheron. “Assessment of Missense Alterations in MLH1 and their Pathogenic Significance.” 2010. Doctoral Dissertation, University of Toronto. Accessed September 19, 2020. http://hdl.handle.net/1807/32048.

MLA Handbook (7th Edition):

Perera, Needra Sheron. “Assessment of Missense Alterations in MLH1 and their Pathogenic Significance.” 2010. Web. 19 Sep 2020.

Vancouver:

Perera NS. Assessment of Missense Alterations in MLH1 and their Pathogenic Significance. [Internet] [Doctoral dissertation]. University of Toronto; 2010. [cited 2020 Sep 19]. Available from: http://hdl.handle.net/1807/32048.

Council of Science Editors:

Perera NS. Assessment of Missense Alterations in MLH1 and their Pathogenic Significance. [Doctoral Dissertation]. University of Toronto; 2010. Available from: http://hdl.handle.net/1807/32048

.